Basic information Safety Supplier Related

4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER

Basic information Safety Supplier Related

4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER Basic information

Product Name:
4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER
Synonyms:
  • 4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER
  • METHYL 4-BENZYLOXYPHENYLACETATE
  • methyl 2-(4-(benzyloxy)phenyl)acetate
  • Benzeneacetic acid, 4-(phenylmethoxy)-, methyl ester
  • methyl 2-(4-phenylmethoxyphenyl)acetate
  • 4-Benzyloxyphenylacetic Acid Methyl Ester,>97%
CAS:
68641-16-7
MF:
C16H16O3
MW:
256.3
Product Categories:
  • Aromatic Esters
Mol File:
68641-16-7.mol
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4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER Chemical Properties

Melting point:
53 °C
Boiling point:
375.0±22.0 °C(Predicted)
Density 
1.129±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to light yellow Solid
CAS DataBase Reference
68641-16-7(CAS DataBase Reference)
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4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER Usage And Synthesis

Synthesis

14199-15-6

100-44-7

68641-16-7

To a suspension of acetone (50 mL) containing potassium carbonate (K2CO3, 20.7 g, 150 mmol) was sequentially added methyl 4-hydroxyphenylacetate (5.0 g, 30 mmol) and benzyl chloride (10.4 mL, 90 mmol). The reaction mixture was heated to reflux for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature, filtered to remove insoluble solids and the filtrate was concentrated. The residue was purified by silica gel column chromatography with 10% ethyl acetate/hexane as eluent to afford methyl 4-benzyloxyphenylacetate (7.7 g, 100% yield) as a white solid. Its 1H NMR (300 MHz, CDCl3) data were as follows: δ 7.40 (m, 5H), 7.21 (d, J = 6.6 Hz, 2H), 6.95 (d, J = 6.6 Hz, 2H), 5.05 (s, 2H), 3.70 (s, 3H), 3.59 (s, 2H).

References

[1] Patent: EP1218005, 2004, B1. Location in patent: Page 26
[2] Patent: WO2014/69963, 2014, A1. Location in patent: Paragraph 464-466
[3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 4, p. 1209 - 1213
[4] Journal of Organic Chemistry, 1982, vol. 47, # 15, p. 2846 - 2851
[5] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 4, p. 525 - 528

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